BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

278 related articles for article (PubMed ID: 4050866)

  • 1. Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother.
    Fujimoto A; Lin MS; Korula SR; Wilson MG
    Am J Med Genet; 1985 Oct; 22(2):333-42. PubMed ID: 4050866
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Trisomy 14 mosaicism: case report and review.
    Johnson VP; Aceto T; Likness C
    Am J Med Genet; 1979; 3(4):331-9. PubMed ID: 474633
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH
    Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
    Wang JC; Mamunes P; Kou SY; Schmidt J; Mao R; Hsu WT
    Am J Med Genet; 1998 Dec; 80(4):418-22. PubMed ID: 9856575
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q.
    Verma RS; Dosik H; Wexler IB
    J Genet Hum; 1977 Dec; 25(4):295-301. PubMed ID: 599332
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
    Cohen MM; Ornoy A; Rosenmann A; Kohn G
    Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Natural history of mosaic trisomy 14 syndrome.
    Fujimoto A; Allanson J; Crowe CA; Lipson MH; Johnson VP
    Am J Med Genet; 1992 Sep; 44(2):189-96. PubMed ID: 1456290
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11).
    Fryns JP; Casaer P; Van den Berghe H
    Hum Genet; 1979 Jan; 46(2):237-41. PubMed ID: 422207
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)].
    Raoul O; Rethoré MO; Dutriliaux B; Michon L; Lejeune J
    Ann Genet; 1975 Mar; 18(1):35-9. PubMed ID: 1080036
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11).
    Rosenmann A; Isacson M; Cohen R; Segal M; Cohen MM
    Ann Genet; 1978 Mar; 21(1):60-4. PubMed ID: 308346
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Skin pigment anomalies and mosaicism for a double autosomal trisomy (48,XX,+18,+20).
    Devriendt K; Matthijs G; Meireleire J; Roelen L; van Buggenhout G; Fryns JP
    Genet Couns; 1998; 9(4):283-6. PubMed ID: 9894166
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Trisomy of the distal 15q region due to familial balanced translocation t(15;16)(q24;p13) and unusual mosaicism in the mother of the proband].
    Nazarenko SA; Nazarenko LP; Baranova VA
    Tsitol Genet; 1987; 21(6):434-7. PubMed ID: 3445362
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter).
    Delaroche I; Bruni L; Giannotti A; Giampaolo R; Aebischer ML
    Helv Paediatr Acta; 1984 May; 39(2):161-6. PubMed ID: 6543839
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
    Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Mosaic 14 trisomy in a female child with multiple abnormalities].
    Rethoré MO; Couturier J; Carpentier S; Ferrand J; Lejeune J
    Ann Genet; 1975 Mar; 18(1):71-4. PubMed ID: 1080041
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations.
    Wilson WG; Shires MA; Willson KA; Wyandt HE; Harris LM; Kelly TE
    Am J Med Genet; 1983 Sep; 16(1):131-6. PubMed ID: 6638063
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12).
    Gonzalez CH; Billerbeck AE; Takayama LC; Wajntal A
    Am J Med Genet; 1983 Jan; 14(1):159-67. PubMed ID: 6829605
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-inactivation pattern in three cases of X/autosome translocation.
    Zabel BU; Baumann WA; Pirntke W; Gerhard-Ratschow K
    Am J Med Genet; 1978; 1(3):309-17. PubMed ID: 677170
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trisomy 20pter = to q11 in a malformed boy from a t(13;20)(p11;q11) translocation-carrier mother.
    Schinzel A
    Hum Genet; 1980 Feb; 53(2):169-72. PubMed ID: 7358383
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 46,X,i(Xq)/47,XX,+13 mosaicism.
    Igarashi M; Tsukahara M; Sugio Y; Katayama K; Kajii T
    Ann Genet; 1985; 28(4):241-4. PubMed ID: 3879438
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.